40795-02-6

Basic information

• Product Name: 3-methyl-2-(4-nitrophenyl)-1,3-oxazolidine
• Synonyms: Oxazolidine, 3-methyl-2-(4-nitrophenyl)-
• CAS NO: 40795-02-6
• Molecular Formula: C₁₀H₁₂N₂O₃
• Molecular Weight: 208.2139
• Mol File: 40795-02-6.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 325.9°C at 760 mmHg
• Flash Point: 150.9°C
• Density: 1.247g/cm³
• Vapor Pressure: 0.000224mmHg at 25°C
• Refractive Index: 1.569
• PKA: 5.96±0.40(Predicted)
• CAS DataBase Reference: 3-methyl-2-(4-nitrophenyl)-1,3-oxazolidine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-methyl-2-(4-nitrophenyl)-1,3-oxazolidine(40795-02-6)
• EPA Substance Registry System: 3-methyl-2-(4-nitrophenyl)-1,3-oxazolidine(40795-02-6)

Safety Data

• Hazardous Substances Data: 40795-02-6(Hazardous Substances Data)

Upstream product

• 109-83-1 (2-hydroxyethyl)(methyl)amine 
• 555-16-8 4-nitrobenzaldehdye 

Downstream Products

• 131602-86-3 2-Methyl-6-(4-nitro-phenyl)-[1,5,2]dioxazinane 
• 131602-78-3 3-Methyl-2-(4-nitro-phenyl)-oxazolidine 3-oxide 

Relevant articles and documents

Isocyanide based multicomponent reactions of oxazolidines and related systems

N-Alkyloxazolidines react in a multicomponent reaction with carboxylic acids and isocyanides to give N-acyloxyethylamino acid amides. The previously reported reaction conditions were improved using a design of experiments approach (DoE). Under the optimis

Synthesis of N-(dialkylaminoalkyl)alcohols by homogeneously catalyzed hydrogenolysis of cyclic N,O-acetals

The homogeneously catalyzed hydrogenation of 1,3-oxazolidines affording unsymmetrically substituted 2-N-(dialkylamino)ethanols is reported showing for the first time that Rh(I) catalysts based on chelating diphosphines can be advantageous for this reaction.

Comparative radioprotective activity of various pentagonal compounds with two heteroatomes

Various heterocyclic compounds with two heteroatomes were synthesized and their potential radioprotective activity was tested. This study shows the interest of phenylthiazolidines derivatives in chemical radioprotection.